The Genotype-Tissue Expression (GTEx) pilot analysis: Multitissue gene regulation in humans
Open accessAbstract
Expression, genetic variation, and tissues: Human genomes show extensive genetic variation across individuals, but we have only just started documenting the effects of this variation on the regulation of gene expression. Furthermore, only a few tissues have been examined per genetic variant. In order to examine how genetic expression varies among tissues within individuals, the Genotype-Tissue Expression (GTEx) Consortium collected 1641 postmortem samples covering 54 body sites from 175 individuals. They identified quantitative genetic traits that affect gene expression and determined which of these exhibit tissue-specific expression patterns. Melé et al. measured how transcription varies among tissues, and Rivas et al. looked at how truncated protein variants affect expression across tissues. Science , this issue p. 648 , p. 660 , p. 666 ; see also p. 640
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For the second stage of vision-language alignment (stage 3 of TITAN), a dataset of 182,862 slide-report pairs was curated from in-house clinical reports and pathology notes from the GTEx consortium.
“For the second stage of vision-language alignment (stage 3 of TITAN), we curated a dataset of 182,862 slide-report pairs from a combination of in-house clinical reports and pathology notes from the GTEx consortium129.”
From A multimodal whole-slide foundation model for pathology (2025) · cites this paper as [129]
The Study design section identifies GTEx as a source of human tissue samples, supporting the identification of the consortium. Our copy does not mention pathology notes or establish that they were available for the citing authors’ slide-report pairs. The dataset curation and pair count are presented as the citing authors’ own work, not as findings of this source. (LLM, conf=0.76)
Experimental — accuracy not yet measuredLarge consortia projects (GTEx, Epigenome Roadmap, ENCODE) are already generating data from multiple-omics levels that facilitate integrated analyses.
“Projects from large consortia like GTEx [156], the Epigenome Roadmap [176] and ENCODE [15] are already generating data from multiple-omics levels that facilitate these integrated analyses.”
From Gene co-expression analysis for functional classification and gene–disease predictions (2017) · cites this paper as [156]
NaV1.2 is widely expressed throughout the human central nervous system but not in peripheral tissues.
“NaV1.2 is widely expressed throughout the human central nervous system, but not in peripheral tissues [7,8].”
From Progress in Understanding and Treating SCN2A-Mediated Disorders (2018) · cites this paper as [7]
The “Gene expression across tissues” section describes broad expression patterns across brain and other tissues, but does not report NaV1.2 expression. Searches for “NaV1.2,” “SCN2A,” and the claimed CNS-versus-peripheral pattern found no passage addressing that specific claim. (LLM, conf=0.76)
Experimental — accuracy not yet measuredRegulatory relationships between non-coding variants and their target genes vary across human cell types, tissues, developmental stages, and species.
“Such regulatory relationships show substantial heterogeneity across human cell types, tissues, and developmental stages (10), and are often highly species-specific (11).”
From Transcriptome-wide isoform-level dysregulation in ASD, schizophrenia, and bipolar disorder (2018) · cites this paper as [10]
GTEx data show multiple eQTLs within these enhancers associated with alterations in SCN1A expression in humans.
“Corroborating this hypothesis, GTEx data show multiple eQTLs within these enhancers that are associated with alterations in SCN1A expression in humans49.”
From Viral manipulation of functionally distinct interneurons in mice, non-human primates and humans (2020) · cites this paper as [49]
Strong significant associations (FDR<0.05) were found between a SNP and expression of nearby genes in subcutaneous adipose tissues.
“We found strong significant associations (false discovery rate (FDR)<0.05) between a SNP and expression of nearby genes in subcutaneous adipose tissues (Supplementary Data 13).”
From Meta-analysis identifies five novel loci associated with endometriosis highlighting key genes involved in hormone metabolism (2017) · cites this paper as [29]
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Self-citationAbundant contribution of short tandem repeats to gene expression variation in humans
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The Dynamic Landscape of Open Chromatin during Human Cortical Neurogenesis
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Tissue-specific regulatory circuits reveal variable modular perturbations across complex diseases
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A compendium of promoter-centered long-range chromatin interactions in the human genome
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Oxytocin pathway gene networks in the human brain
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Self-citation
- Authors
- The GTEx Consortium, Ardlie, K. G., Deluca, D. S., Segrè, A. V., Sullivan, T. J., Young, T. R., Gelfand, E. T., Trowbridge, C. A., Maller, J. B., Tukiainen, T., Lek, M., Ward, L. D., Kheradpour, P., Iriarte, B., Meng, Y., Palmer, C. D., Esko, T., Winckler, W., Hirschhorn, J. N., Kellis, M., MacArthur, D. G., Getz, G., Shabalin, A. A., Li, G., Zhou, Y.-H., Nobel, A. B., Rusyn, I., Wright, F. A., Lappalainen, T., Ferreira, P. G., Ongen, H., Rivas, M. A., Battle, A., Mostafavi, S., Monlong, J., Sammeth, M., Mele, M., Reverter, F., Goldmann, J. M., Koller, D., Guigó, R., McCarthy, M. I., Dermitzakis, E. T., Gamazon, E. R., Im, H. K., Konkashbaev, A., Nicolae, D. L., Cox, N. J., Flutre, T., Wen, X., Stephens, M., Pritchard, J. K., Tu, Z., Zhang, B., Huang, T., Long, Q., Lin, L., Yang, J., Zhu, J., Liu, J., Brown, A., Mestichelli, B., Tidwell, D., Lo, E., Salvatore, M., Shad, S., Thomas, J. A., Lonsdale, J. T., Moser, M. T., Gillard, B. M., Karasik, E., Ramsey, K., Choi, C., Foster, B. A., Syron, J., Fleming, J., Magazine, H., Hasz, R., Walters, G. D., Bridge, J. P., Miklos, M., Sullivan, S., Barker, L. K., Traino, H. M., Mosavel, M., Siminoff, L. A., Valley, D. R., Rohrer, D. C., Jewell, S. D., Branton, P. A., Sobin, L. H., Barcus, M., Qi, L., McLean, J., Hariharan, P., Um, K. S., Wu, S., Tabor, D., Shive, C., Smith, A. M., Buia, S. A., Undale, A. H., Robinson, K. L., Roche, N., Valentino, K. M., Britton, A., Burges, R., Bradbury, D., Hambright, K. W., Seleski, J., Korzeniewski, G. E., Erickson, K., Marcus, Y., Tejada, J., Taherian, M., Lu, C., Basile, M., Mash, D. C., Volpi, S., Struewing, J. P., Temple, G. F., Boyer, J., Colantuoni, D., Little, R., Koester, S., Carithers, L. J., Moore, H. M., Guan, P., Compton, C., Sawyer, S. J., Demchok, J. P., Vaught, J. B., Rabiner, C. A., Lockhart, N. C., Ardlie, K. G., Getz, G., Wright, F. A., Kellis, M., Volpi, S., & Dermitzakis, E. T.
- Affiliations
- Amélioration Génétique et Adaptation des Plantes méditerranéennes et tropicales (FR)
- ORCID
- Deluca, David S.
- Segrè, Ayellet V.
- Young, Taylor R.
- Maller, Julian B.
- Tukiainen, Taru
- Lek, Monkol
- Ward, Lucas D.
- Meng, Yan
- Palmer, Cameron D.
- Esko, Tõnu
- Winckler, Wendy
- Hirschhorn, Joel N.
- MacArthur, Daniel G.
- Shabalin, Andrey A.
- Li, Gen
- Zhou, Yi-Hui
- Nobel, Andrew B.
- Rusyn, Ivan
- Lappalainen, Tuuli
- Ferreira, Pedro G.
- Ongen, Halit
- Rivas, Manuel A.
- Battle, Alexis
- Mostafavi, Sara
- Monlong, Jean
- Sammeth, Michael
- Goldmann, Jakob M.
- Guigó, Roderic
- McCarthy, Mark I.
- Gamazon, Eric R.
- Im, Hae Kyung
- Konkashbaev, Anuar
- Nicolae, Dan L.
- Cox, Nancy J.
- Flutre, Timothée
- Wen, Xiaoquan
- Stephens, Matthew
- Pritchard, Jonathan K.
- Tu, Zhidong
- Zhang, Bin
- Huang, Tao
- Long, Quan
- Lin, Luan
- Yang, Jialiang
- Zhu, Jun
- Moser, Michael T.
- Gillard, Bryan M.
- Choi, Christopher
- Foster, Barbara A.
- Mosavel, Maghboeba
- Siminoff, Laura A.
- Rohrer, Daniel C.
- Jewell, Scott D.
- Branton, Philip A.
- Tabor, David
- Lu, Chunrong
- Mash, Deborah C.
- Struewing, Jeffery P.
- Moore, Helen M.
- Compton, Carolyn
- Sawyer, Sherilyn J.
- Venue
- Science
- Published
- 2015-05-08
- Volume
- 348
- Issue
- 6235
- Pages
- 648-660
- ISSN
- 0036-8075 (ISSN-L)
- 1095-9203
- PMC
- PMC4547484
- OpenAlex
- W1533942137
- Cited by
- 5,062
- References
- 83
- Citations by year
- 2026: 171 · 2025: 315 · 2024: 417 · 2023: 385 · 2022: 417 · 2021: 621 · 2020: 587 · 2019: 516 · 2018: 610 · 2017: 516 · 2016: 398 · 2015: 103 · 2014: 2 · 2013: 1
- FWCI
- 371.27
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Locations
- Science (publishedVersion)
- PubMed (publishedVersion)
- PubMed Central (acceptedVersion)
- Carolina Digital Repository (University of North Carolina at Chapel Hill) (submittedVersion)
- HAL (submittedVersion)
- UNC Libraries
- Funders
- U.S. National Institutes of Health
- NIH (HHSN261200800001E, R01 DA006227-17, R01 MH090941, R01 MH090951, R01 MH090937, R01 MH090936, R01 MH090948, R01 GM104371, R01AG046170, R01CA163772, U01AI111598-01)
- NIMH
- NIDA
- NIA
- NHLBI
- NHGRI
- NCI
- NIAID
- NINDS
- Office of the Director
- Roswell Park Cancer Institute (10XS171)
- Wellcome Trust (98381)
- European Research Council
- Louis-Jeantet Foundation
- Swiss National Science Foundation
- NDRI (10XS170)
- Science Care Inc. (10X172)
- IDOX (12ST1039)
- Van Andel Institute (10ST1035)
- Broad Institute (HHSN268201000029C)
- Clarendon Scholarship
- NDM Studentship
- Univ. of Oxford Green Templeton College Award
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Genetic Associations and Epidemiology
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Genomics and Chromatin Dynamics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › RNA Research and Splicing
- Keywords
- gene expression, tissue-specific gene regulation, expression quantitative trait loci, human genetic variation, regulatory networks, genome-wide association study, GTEx, RNA sequencing, tissue heterogeneity
- MeSH terms
- Alleles, Blood Pressure, Disease, Gene Expression Regulation, Multigene Family, Genotype, Humans, Organ Specificity, Pilot Projects, RNA Splicing, Genetic Variation, Genome, Human, Tibial Arteries, Sequence Analysis, RNA, GTPase-Activating Proteins, RNA, Untranslated, Quantitative Trait Loci, Gene Regulatory Networks, Genome-Wide Association Study, Transcriptome
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